7-oxo-pyridopyrimidines (II)

ABSTRACT

The present invention provides compounds of the formula:  
                 
 
     a prodrug or a pharmaceutically acceptable salt thereof, wherein R 1 , R 2 , R 3  and Ar 1  are those defined herein, and methods for preparation and uses thereof.

CROSS-REFERENCE TO RELATED APPLICATIONS

[0001] This application claims the benefit of U.S. ProvisionalApplication Nos. 60/229,584, filed Aug. 31, 2000 and 60/229,577, filedAug. 31, 2000, which are incorporated herein by reference in theirentirety. This patent application also incorporates by reference theentire disclosure of U.S. patent application Ser. No. ______ entitled7-Oxo-Pyridopyrimidines (I) by inventors Jeffrey Chen, James Dunn, DavidGoldstein and Julie Lim, filed concurrently on Aug. 30, 2001, which isfurther identified as Attorney Docket Number R0094B.

FIELD OF THE INVENTION

[0002] The present invention relates to 7-oxo-pyridopyrimidines. Inparticular, the present invention provides 2,6-disubstituted7-oxo-pyrido[2,3-d]pyrimidines, a process for their manufacture,pharmaceutical preparations comprising the same, and methods for usingthe same.

BACKGROUND OF THE INVENTION

[0003] Mitogen-activated protein kinases (MAP) is a family ofproline-directed serine/threonine kinases that activate their substratesby dual phosphorylation. The kinases are activated by a variety ofsignals including nutritional and osmotic stress, UV light, growthfactors, endotoxin and inflammatory cytokines. One group of MAP kinasesis the p38 kinase group which includes various isoforms (e.g., p38α,p39β, p38γ and p38δ). The p38 kinases are responsible forphosphorylating and activating transcription factors as well as otherkinases, and are activated by physical and chemical stress,pro-inflammatory cytokines and bacterial lipopolysaccharide.

[0004] More importantly, the products of the p38 phosphorylation havebeen shown to mediate the production of inflammatory cytokines,including TNF and IL-1, and cyclooxygenase-2. Each of these cytokineshas been implicated in numerous disease states and conditions. Forexample, TNF-α is a cytokine produced primarily by activated monocytesand macrophages. Its excessive or unregulated production has beenimplicated as playing a causative role in the pathogenesis of rheumatoidarthritis. More recently, inhibition of TNF production has been shown tohave broad application in the treatment of inflammation, inflammatorybowel disease, multiple sclerosis and asthma.

[0005] TNF has also been implicated in viral infections, such as HIV,influenza virus, and herpes virus including herpes simplex virus type-1(HSV-1), herpes simplex virus type-2 (HSV-2), cytomegalovirus (CMV),varicella-zoster virus (VZV), Epstein-Barr virus, human herpes virus-6(HHV-6), human herpesvirus-7 (HHV-7), human herpesvirus-8 (HHV-8),pseudorabies and rhinotracheitis, among others.

[0006] Similarly, IL-1 is produced by activated monocytes andmacrophages, and plays a role in many pathophysiological responsesincluding rheumatoid arthritis, fever and reduction of bone resorption.

[0007] Additionally, the involvement of p38 has been implicated instroke, Alzheimer's disease, osteoarthritis, lung injury, septic shock,angiogenesis, dermatitis, psoriasis and atopic dermatitis. J. Exp. Opin.Ther. Patents, (2000) 10(1).

[0008] Certain pyrido[2,3-d]pyrimidines are disclosed as inhibitors ofprotein tyrosine kinase mediated cellular proliferation in WO 96/34867,published Nov. 7, 1996 (Warner Lambert).

[0009] The inhibition of these cytokines by inhibition of the p38 kinaseis of benefit in controlling, reducing and alleviating many of thesedisease states.

SUMMARY OF THE INVENTION

[0010] One aspect of the present invention provides compoundsrepresented by the Formula:

[0011] a prodrug or a pharmaceutically acceptable salt thereof, inwhich:

[0012] R¹ is hydrogen or alkyl;

[0013] R² is —CR′R″—R^(a) (where R′ and R″ are hydrogen, hydroxyalkyl oralkyl with at least one being alkyl or hydroxyalkyl and R^(a) ishydroxyalkyl), R^(x)—S—R^(y)— (where R^(x) is alkyl and R^(y) isalkylene), alkoxy-substituted alkyl , heterocyclylalkyl or C₄-C₅cycloalkyl, wherein each of the hydroxy group present in R² can beindependently in the form of an ester, a carbamate, a carbonate, or asulfonate derivative; or

[0014] R¹ and R² together with the nitrogen atom to which they areattached form aheterocyclyl group;

[0015] R³ is hydrogen, alkyl, cycloalkyl, aryl, aralkyl, haloalkyl,heteroalkyl, cyanoalkyl, amino, monoalkylamino, dialkylamino,alkylene-C(O)—R (where R is hydrogen, alkyl, hydroxy, alkoxy, amino,monoalkylamino or dialkylamnino) or acyl; and

[0016] Ar¹ is aryl.

[0017] The compounds of Formula I and their aforementioned salts areinhibitors of protein kinases, and exhibit effective activity againstp38 in vivo. Therefore, the compounds can be used for the treatment ofdiseases mediated by the pro-inflammatory cytokines such as TNF andIL-1.

[0018] Thus, another aspect of the present invention provides methodsfor the treatment of p38 mediated diseases or conditions in which atherapeutically effective amount of a compound of Formula I isadministered to a patient in need of such treatment.

[0019] Yet another aspect of the present invention provides methods forpreparing the compounds described above.

[0020] Still yet another aspect of the present invention providesmethods for preparing medicaments useful for the treatment of the p38mediated diseases and conditions.

DEFINITIONS

[0021] Unless otherwise stated, the following terms used in thespecification and claims have the meanings given below:

[0022] “Acyl” means a radical —C(O)R, where R is hydrogen, alkyl,cycloalkyl, cycloalkylalkyl, phenyl or phenylalkyl wherein alkyl,cycloalkyl, cycloalkylalkyl, and phenylalkyl are as defined herein.Representative examples include, but are not limited to formyl, acetyl,cylcohexylcarbonyl, cyclohexylmethylcarbonyl, benzoyl, benzylcarbonyl,and the like. “Acylamino” means a radical —NR′C(O)R, where R′ ishydrogen or alkyl, and R is hydrogen, alkyl, cycloalkyl,cycloalkylalkyl, phenyl or phenylalkyl wherein alkyl, cycloalkyl,cycloalkylalkyl, and phenylalkyl are as defined herein. Representativeexamples include, but are not limited to formylamino, acetylamino,cylcohexylcarbonylamino, cyclohexylmethyl-carbonylamino, benzoylamino,benzylcarbonylamino, and the like.

[0023] “Alkoxy” means a radical —OR where R is an alkyl as definedherein e.g., methoxy, ethoxy, propoxy, butoxy and the like. “Alkyl”means a linear saturated monovalent hydrocarbon radical of one to sixcarbon atoms or a branched saturated monovalent hydrocarbon radical ofthree to six carbon atoms, e.g., methyl, ethyl, propyl, 2-propyl,n-butyl, iso-butyl, tert-butyl, pentyl, and the like.“Alkylene” means alinear saturated divalent hydrocarbon radical of one to six carbon atomsor a branched saturated divalent hydrocarbon radical of three to sixcarbon atoms, e.g., methylene, ethylene, 2,2-dimethylethylene,propylene, 2-methylpropylene, butylene, pentylene, and the like.

[0024] “Alkylthio” means a radical —SR where R is an alkyl as definedabove e.g., methylthio, ethylthio, propylthio, butylthio, and the like.

[0025] “Aryl” means a monovalent monocyclic or bicyclic aromatichydrocarbon radical which is optionally substituted independently withone or more substituents, preferably one, two or three, substituentspreferably selected from the group consisting of alkyl, hydroxy, alkoxy,haloalkyl, haloalkoxy, heteroalkyl, halo, nitro, cyano, amino,monoalkylamino, dialkylamino, methylenedioxy, ethylenedioxy and acyl.More specifically the term aryl includes, but is not limited to, phenyl,chlorophenyl, fluorophenyl, methoxyphenyl, 1-naphthyl, 2-naphthyl, andthe derivatives thereof.

[0026] “Cycloalkyl” refers to a saturated monovalent cyclic hydrocarbonradical of three to seven ring carbons e.g., cyclopropyl, cyclobutyl,cyclohexyl, 4-methylcyclohexyl, and the like.

[0027] “Cycloalkylalkyl” means a radical —R^(a)R^(b) where R^(a) is analkylene group and R^(b) is cycloalkyl group as defined herein, e.g.,cyclohexylmethyl, and the like.

[0028] “Dialkylamino” means a radical —NRR′ where R and R′ independentlyrepresent an alkyl, hydroxyalkyl, cycloalkyl, or cycloalkylalkyl groupas defined herein. Representative examples include, but are not limitedto dimethylamino, methylethylamino, di(l-methylethyl)amino,(cyclohexyl)(methyl)amino, (cyclohexyl)(ethyl)amino,(cyclohexyl)(propyl)amino, (cyclohexylmethyl)(methyl)amino,(cyclohexylmethyl)(ethyl)amino, and the like.

[0029] The term “each of the hydroxy group present in R² can beindependently in the form of an ester, a carbamate, a carbonate or asulfonate derivative” means that hydroxy group(s) (—OH) which arepresent in the R² group can be independently derivatized asR^(a)—C(═O)—O—, R^(a)R^(b)N—C(═O)—O—, R^(a)—O—C(═O)—O— or R^(a)—SO₂—O—,respectively, where R^(a) and R^(b) is independently hydrogen, alkyl,aryl or aralkyl as defined herein.

[0030] “Halo” means fluoro, chloro, bromo, or iodo, preferably fluoroand chloro.

[0031] “Haloalkyl” means alkyl substituted with one or more same ordifferent halo atoms, e.g., —CH₂Cl, —CF₃, —CH₂CF₃, —CH₂CCl₃, and thelike.

[0032] “Heteroalkyl” means an alkyl radical as defined herein whereinone, two or three hydrogen atoms have been replaced with a substituentindependently selected from the group consisting of —OR^(a),—NR^(b)R^(c), and —S(O)_(n)R^(d) (where n is an integer from 0 to 2),with the understanding that the point of attachment of the heteroalkylradical is through a carbon atom, wherein Ra is hydrogen, acyl, alkyl,cycloalkyl, or cycloalkylalkyl; R^(b) and R^(c) are independently ofeach other hydrogen, acyl, alkyl, cycloalkyl, or cycloalkylalkyl, orR^(b) and R^(c) together forms cycloalkyl or arylcycloalkyl; and when nis 0, R^(d) is hydrogen, alkyl, cycloalkyl, or cycloalkylalkyl, and whenn is 1 or 2, R^(d) is alkyl, cycloalkyl, cycloalkylalkyl, amino,acylamino, monoalkylamino, or dialkylamino. Representative examplesinclude, but are not limited to, 2-hydroxyethyl, 3-hydroxypropyl,2-hydroxy-1-hydroxymethylethyl, 2,3-dihydroxypropyl,1-hydroxymethylethyl, 3-hydroxybutyl, 2,3-dihydroxybutyl,2-hydroxy-1-methylpropyl, 2-aminoethyl, 3-aminopropyl,2-methylsulfonylethyl, aminosulfonylmethyl, aminosulfonylethyl,aminosulfonylpropyl, methylaminosulfonylmethyl,methylarninosulfonylethyl, methylaminosulfonylpropyl, and the like.

[0033] “Heteroalkylsubstituted cycloalkyl” means a cycloalkyl radical asdefined herein wherein one, two or three hydrogen atoms in thecycloalkyl radical have been replaced with a heteroalkyl group with theunderstanding that the heteroalkyl radical is attached to the cycloalkylradical via a carbon-carbon bond. Representative examples include, butare not limited to, 1-hydroxymethylcyclopentyl,2-hydroxymethylcyclohexyl, and the like.

[0034] “Heterosubstituted cycloalkyl” means a cycloalkyl radical asdefined herein wherein one, two or three hydrogen atoms in thecycloalkyl radical have been replaced with a substituent independentlyselected from the group consisting of hydroxy, alkoxy, amino, acylamino,monoalkylamino, dialkylamino, oxo (C═O), imino, hydroximino (═NOH),NR′SO₂R^(d) (where R′ is hydrogen or alkyl and R is alkyl, cycloalkyl,amino, monoalkylamino or dialkylamino), —X—C(O)R (where X is O or NR′, Ris hydrogen, alkyl, haloalkyl, alkoxy, amino, monoalkylamino,dialkylamino, or optionally substituted phenyl, and R′ is H or alkyl),or —S(O)_(n)R (where n is an integer from 0 to 2) such that when n is 0,R is hydrogen, alkyl, cycloalkyl, or cycloalkylalkyl, and when n is 1 or2, R is alkyl, cycloalkyl, cycloalkylalkyl, amino, acylamino,monoalkylamino or dialkylamino. Representative examples include, but arenot limited to, 2-, 3-, or 4-hydroxycyclohexyl, 2-, 3-, or4-aminocyclohexyl, 2-, 3-, or 4-methanesulfonamido-cyclohexyl, and thelike, preferably 4-hydroxycyclohexyl, 2-aminocyclohexyl,4-methanesulfonamido-cyclohexyl.

[0035] “Heterosubstituted cycloalkyl-alkyl” means a radical R^(a)R^(b)where R^(a) is a heterosubstituted cycloalkyl radical and R^(b) is analkylene radical.

[0036] “Heterocyclyl” means a saturated or unsaturated non-aromaticcyclic radical of 3 to 8 ring atoms in which one or two ring atoms areheteroatoms selected from N, O, or S(O)_(n) (where n is an integer from0 to 2), the remaining ring atoms being C. The heterocyclyl ring may beoptionally substituted independently with one, two, three or foursubstituents selected from alkyl, haloalkyl, heteroalkyl, halo, nitro,cyano, cyanoalkyl, hydroxy, alkoxy, amino, monoalkylamino, dialkylamino,aralkyl, —(X)_(n)—C(O)R (where, X is O or NR′, n is 0 or 1, R ishydrogen, alkyl, haloalkyl, hydroxy (when n is 0), alkoxy, amino,monoalkylamino, dialkylamino or optionally substituted phenyl, and R′ isH or alkyl),-alkylene-C(O)R (where R is OR or NR′R″ and R is hydrogen,alkyl or haloalkyl, and R′ and R″ are independently hydrogen or alkyl),—alkylene—(O)_(n)—R^(a) (where n is 0, 1 or 2, preferably 0, and R^(a)is alkyl) or —S(O)_(n)R (where n is an integer from 0 to 2) such thatwhen n is 0, R is hydrogen, alkyl, haloalkyl, cycloalkyl, orcycloalkylalkyl, and when n is 1 or 2, R is alkyl, cycloalkyl,cycloalkylalkyl, amino, acylamino, monoalkylamino or dialkylamino. Morespecifically the term heterocyclyl includes, but is not limited to,tetrahydropyranyl, piperidino, N-methylpiperidin-3-yl, piperazino,N-methylpyrrolidin-3-yl, 3-pyrrolidino, morpholino, thiomorpholino,thiomorpholino-1-oxide, thiomorpholino-1,1-dioxide, pyrrolinyl,imidazolinyl, N-methanesulfonyl-piperidin-4-yl, and the derivativesthereof. “Heterocyclylalkyl” means a radical —R^(a)R^(b) where Ra is analkylene group and R^(b) is a heterocyclyl group as defined above withthe understanding that R^(b) is attached to R^(a) via a carbon atom ofthe heterocyclyl ring, e.g., tetrahydropyran-2-ylmethyl, 2- or3-piperidinylmethyl, and the like.

[0037] “Hydroxyalkyl” means an alkyl radical as defined herein,substituted with one or more, preferably one, two or three hydroxygroups, provided that the same carbon atom does not carry more than onehydroxy group. Representative examples include, but are not limited to,hydroxymethyl, 2-hydroxyethyl, 2-hydroxypropyl, 3-hydroxypropyl,1-(hydroxymethyl)-2-methylpropyl, 2-hydroxybutyl, 3-hydroxybutyl,4-hydroxybutyl, 2,3-dihydroxypropyl, 2-hydroxy-1-hydroxymethylethyl,2,3-dihydroxybutyl, 3,4-dihydroxybutyl and2-(hydroxymethyl)-3-hydroxypropyl, preferably 2-hydroxyethyl,2,3-dihydroxypropyl and 1-(hydroxymethyl)-2-hydroxyethyl. Accordingly,as used herein, the term “hydroxyalkyl” is used to define a subset ofheteroalkyl groups.

[0038] “Leaving group” has the meaning conventionally associated with itin synthetic organic chemistry, i.e., an atom or a group capable ofbeing displaced by a nucleophile and includes halo (such as chloro,bromo, and iodo), alkanesulfonyloxy, arenesulfonyloxy, alkylcarbonyloxy(e.g., acetoxy), arylcarbonyloxy, mesyloxy, tosyloxy,trifluoromethanesulfonyloxy, aryloxy (e.g., 2,4-dinitrophenoxy),methoxy, N,O -dimethylhydroxylamino, and the like.

[0039] “Monoalkylamino” means a radical —NHR where R is an alkyl,hydroxyalkyl, cycloalkyl, or cycloalkylalkyl group as defined above,e.g., methylamino, (1-methylethyl)amino, hydroxymethylamino,cyclohexylamino, cyclohexylmethylamino, cyclohexylethylamino, and thelike.

[0040] “Optionally substituted phenyl” means a phenyl ring which isoptionally substituted independently with one or more substituents,preferably one or two substituents selected from the group consisting ofalkyl, hydroxy, alkoxy, haloalkyl, haloalkoxy, heteroalkyl, halo, nitro,cyano, amino, methylenedioxy, ethylenedioxy, and acyl.

[0041] “Pharmaceutically acceptable excipient” means an excipient thatis useful in preparing a pharmaceutical composition that is generallysafe, non-toxic and neither biologically nor otherwise undesirable, andincludes excipient that is acceptable for veterinary use as well ashuman pharmaceutical use. A “pharmaceutically acceptable excipient” asused in the specification and claims includes both one and more than onesuch excipient.

[0042] “Pharmaceutically acceptable salt” of a compound means a saltthat is pharmaceutically acceptable and that possesses the desiredpharmacological activity of the parent compound. Such salts include: (1)acid addition salts, formed with inorganic acids such as hydrochloricacid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, andthe like; or formed with organic acids such as acetic acid, propionicacid, hexanoic acid, cyclopentanepropionic acid, glycolic acid, pyruvicacid, lactic acid, malonic acid, succinic acid, malic acid, maleic acid,fumaric acid, tartaric acid, citric acid, benzoic acid,3-(4-hydroxybenzoyl)benzoic acid, cinnamic acid, mandelic acid,methanesulfonic acid, ethanesulfonic acid, 1,2-ethane-disulfonic acid,2-hydroxyethanesulfonic acid, benzenesulfonic acid,4-chlorobenzenesulfonic acid, 2-naphthalenesulfonic acid,4-toluenesulfonic acid, camphorsulfonic acid,4-methylbicyclo[2.2.2]-oct-2-ene-1-carboxylic acid, glucoheptonic acid,3-phenylpropionic acid, trimethylacetic acid, tertiary butylacetic acid,lauryl sulfuric acid, gluconic acid, glutamic acid, hydroxynaphthoicacid, salicylic acid, stearic acid, muconic acid, and the like; or (2)salts formed when an acidic proton present in the parent compound eitheris replaced by a metal ion, e.g., an alkali metal ion, an alkaline earthion, or an aluminum ion; or coordinates with an organic base such asethanolamine, diethanolamine, triethanolamine, tromethamine,N-methylglucamine, and the like.

[0043] The terms “pro-drug” and “prodrug” are used interchangeablyherein and refer to any compound which releases an active parent drugaccording to Formula I in vivo when such prodrug is administered to amammalian subject. Prodrugs of a compound of Formula I are prepared bymodifying one or more functional group(s) present in the compound ofFormula I in such a way that the modification(s) may be cleaved in vivoto release the parent compound. Prodrugs include compounds of Formula Iwherein a hydroxy, amino, sulfhydryl, carboxy or carbonyl group in acompound of Formula I is bonded to any group that may be cleaved in vivoto regenerate the free hydroxyl, amino, or sulfhydryl group,respectively. Examples of prodrugs include, but are not limited to,esters (e.g., acetate, dialkylaminoacetates, formates, phosphates,sulfates, and benzoate derivatives), sulfonates and carbamates (e.g.,N,N-dimethylaminocarbonyl) of hydroxy functional groups, esters groups(e.g. ethyl esters, morpholinoethanol esters) of carboxyl functionalgroups, N-acyl derivatives (e.g. N-acetyl) N-Mannich bases, Schiff basesand enaminones of amino functional groups, oximes, acetals, ketals andenol esters of ketone and aldehyde functional groups in compounds ofFormula I, and the like, See Bundegaard, H. “Design of Prodrugs” p1-92,Elesevier, New York-Oxford (1985).

[0044] “Protecting group” refers to a grouping of atoms that whenattached to a reactive group in a molecule masks, reduces or preventsthat reactivity. Examples of protecting groups can be found in T. W.Green and P. G. Futs, Protective Groups in Organic Chemistry, (Wiley,2nd ed. 1991) and Harrison and Harrison et al., Compendium of SyntheticOrganic Methods, Vols. 1-8 (John Wiley and Sons, 1971-1996).Representative amino protecting groups include, formyl, acetyl,trifluoroacetyl, benzyl, benzyloxycarbonyl (CBZ), tert-butoxycarbonyl(Boc), trimethyl silyl (TMS), 2-trimethylsilyl-ethanesulfonyl (SES),trityl and substituted trityl groups, allyloxycarbonyl,9-fluorenylmethyloxycarbonyl (FMOC), nitro-veratryloxycarbonyl (NVOC),and the like. Representative hydroxy protecting groups include thosewhere the hydroxy group is either acylated or alkylated such as benzyl,and trityl ethers as well as alkyl ethers, tetrahydropyranyl ethers,trialkylsilyl ethers and allyl ethers.

[0045] “Treating” or “treatment” of a disease includes: (1) preventingthe disease, i.e., causing the clinical symptoms of the disease not todevelop in a mammal that may be exposed to or predisposed to the diseasebut does not yet experience or display symptoms of the disease; (2)inhibiting the disease, i.e., arresting or reducing the development ofthe disease or its clinical symptoms; or (3) relieving the disease,i.e., causing regression of the disease or its clinical symptoms.

[0046] “A therapeutically effective amount” means the amount of acompound that, when administered to a mammal for treating a disease, issufficient to effect such treatment for the disease. The“therapeutically effective amount” will vary depending on the compound,the disease and its severity and the age, weight, etc., of the mammal tobe treated.

[0047] The term “treating”, “contacting” or “reacting” when referring toa chemical reaction, means to add or mix two or more reagents underappropriate conditions to produce the indicated and/or the desiredproduct. It should be appreciated that the reaction which produces theindicated and/or the desired product may not necessarily result directlyfrom the combination of two reagents which were initially added, i.e.,there can be one or more intermediates which are produced in the mixturewhich ultimately leads to the formation of the indicated and/or thedesired product.

DETAILED DESCRIPTION

[0048] One aspect of the present invention provides compoundsrepresented by the formula:

[0049] where:

[0050] R¹ is hydrogen or alkyl;

[0051] R² is —CR′R″—R^(a) (where R′ and R″ are hydrogen or alkyl with atleast one being alkyl and R^(a) is hydroxyalkyl), dihydroxyalkyl,R^(x)—S—R^(y) (where R^(x) is alkyl and R^(y) is alkylene),alkoxy-substituted alkyl, heterocyclylalkyl or C₄-C₅ cycloalkyl, whereineach of the hydroxy group present in R² can be independently in the formof an ester, a carbamate, a carbonate, or a sulfonate derivative; or

[0052] R¹ and R2 together with the nitrogen atom to which they areattached form a heterocyclyl group;

[0053] R³ is hydrogen, alkyl, cycloalkyl, aryl, aralkyl, haloalkyl,heteroalkyl, cyanoalkyl, alkylene-C(O)—R (where R is hydrogen, alkyl,hydroxy, alkoxy, amino, monoalkylamino or dialkylamino) or acyl; and

[0054] Ar¹ is aryl.

[0055] Particularly preferred compounds of Formula I are thoserepresented by the Formula II:

[0056] where n is 1 or 2 and X is hydrogen, alkyl, halo, nitro, cyano ormethoxy

[0057] More preferred compounds of Formula I are those represented bythe Formula III:

[0058] In reference to compounds of Formula I:

[0059] Preferably, R¹ is hydrogen or methyl. More preferably, R¹ ishydrogen.

[0060] Preferably, R² of compounds of Formula I is —CR′R″—R^(a) (whereR′ and R″ are hydrogen, hydroxyalkyl or alkyl with at least one beingalkyl or hydroxyalkyl and R^(a) is hydroxyalkyl), alkoxy-substitutedalkyl, or (N-substituted piperidin-4-yl)methyl, wherein each of thehydroxy group present in R² can be independently in the form of anester, a carbamate, a carbonate, or a sulfonate derivative. Morepreferably R² is (1,1-dimethyl-2-hydroxy)ethyl,(1,2-dimethyl-2-hydroxy)propyl, (N-methyl piperidin4-yl)methyl,[1-dimethylacetamido-piperidin4-yl]methyl, [1-carboxymethyl-piperidin-4-yl]methyl, (1,1-dimethyl-2-hydroxy)ethyl, (1-methyl-3-hydroxy)propyl,(1-methyl-1-hydroxymethyl-2-hydroxy)ethyl,[1,1-di(hydroxymethyl)]propyl, (1-hydroxymethyl-2-methyl)propyl,(1-hydroxymethyl)propyl, (1-hydroxymethyl-2,2-dimethyl)propyl,(1-hydroxymethyl-3-methyl)butyl, (2-hydroxy)propyl,(1-methyl-2-hydroxy)ethyl, (1-hydroxymethyl-2-methyl)butyl,2-hydroxyethyl, 2-hydroxy-2-methylpropyl, 5-hydroxypentyl,2-hydroxybutyl, 1-(hydroxymethyl)-2-hydroxyethyl, 2,3-dihydroxypropyl or[1-carbomethoxymethyl-piperidin4-yl]methyl, wherein each of the hydroxygroup present in R² can be independently in the form of an ester, acarbamate, a carbonate, or a sulfonate derivative.

[0061] In another embodiment, preferably R¹ and R² together with thenitrogen atom to which they are attached form -alkylene-S(O)_(n)—R^(a)—substituted heterocyclyl (where n is 0, 1 or 2, preferably 0, and R^(a)is alkyl). More preferably, R¹ and R² together with the nitrogen atom towhich they are attached form -alkylene-S(O)_(n)—R^(a)— substitutedaziridinyl.

[0062] Preferably, R³ of compounds of Formula I is alkyl, amino,monoalkylamino, dialkylamino, haloalkyl, cycloalkyl, cyanomethyl,heteroalkyl, aryl, aralkyl or alkylene-(O)—R (where R is hydrogen,alkyl, hydroxy, alkoxy, amino, monoalkylamino or dialkylamino). Mostpreferably R³ is amino, methyl, 2,2,2-trifluoroethyl, cyclopropyl,cyanomethyl, 2-hydroxyethyl, 4-fluorophenyl, benzyl, carboxymethyl ormethoxycarbonylmethyl. Even more preferably, R³ is methyl.

[0063] It should be appreciated that when R³ is hydrogen, the compoundscan exist in tautomeric form as follows:

[0064] Thus, in addition to the compounds described above, the presentinvention includes all tautomeric forms. Furthermore, the presentinvention also includes all pharmaceutically acceptable salts of thosecompounds along with prodrug forms of the compounds and allstereoisomers whether in a pure chiral form or a racemic mixture orother form of mixture.

[0065] Still further, combinations of the preferred groups describedabove will form other preferred embodiments; thus, for example,preferred substituents R¹, R² and R³ of Formula I are also preferredsubstituents of compounds of Formulas II and III.

[0066] Some of the representative compounds of Formula I are shown inTable 1 below. TABLE 1 Representative compounds of Formula I Cpd #STRUCTURE Melting Point (° C.) Mass spec (MH⁺⁾ 1

228.6-228.9 (salt) 358 2

  220-221.1 (salt) 442 3

235.3-237.9 (salt) 428 4

211.8-212.8 (salt) 455 5

213-220 (salt) 383 6

206.8-207.5 453 7

142.0-149.0 453 8

178.0-181.5 373 9

  194-195.3 373 10

205.3-210.9 11

147-154 12

436.36 13

145.0-163.0 14

200.0-210.0 374 15

 98.1-102.0 388 16

167.1-169.1 372 17

170.5-172.1 358 18

171.2-174.0 386 19

173.1-176.2 386 20

131.1-132.2 344 21

140.1-143.6 386 22

155.8-157.3 360 23

403 24

180.7-189.2 25

>300 26

142.1-144.3 27

156.4-160.2 28

403

[0067] The IC₅₀ of Compounds of Formula I in the in vitro p38 assay isless than 10 μM, preferably less than 5 μM, more preferably less than 2μM, and most preferably less than 1 μM. In particular, Compounds ofFormula I in Table I have IC₅₀ in the in vitro p38 assay of from about0.712 μM to about 0.001 μM.

[0068] The compounds of the present invention can exist in unsolvatedforms as well as solvated forms, including hydrated forms. In general,the solvated forms, including hydrated forms, are equivalent tounsolvated forms and are intended to be encompassed within the scope ofthe present invention. Furthermore, as stated above, the presentinvention also includes all pharmaceutically acceptable salts of thosecompounds along with prodrug forms of the compounds and allstereoisomers whether in a pure chiral form or a racemic mixture orother form of mixture.

[0069] The compounds of Formula I are capable of further formingpharmaceutically acceptable acid addition salts. All of these forms arewithin the scope of the present invention.

[0070] Pharmaceutically acceptable acid addition salts of the compoundsof Formula I include salts derived from inorganic acids such ashydrochloric, nitric, phosphoric, sulfuric, hydrobromic, hydriodic,phosphorus, and the like, as well as the salts derived from organicacids, such as aliphatic mono- and dicarboxylic acids,phenyl-substituted alkanoic acids, hydroxy alkanoic acids, alkanedioicacids, aromatic acids, aliphatic and aromatic sulfonic acids, etc. Suchsalts thus include sulfate, pyrosulfate, bisulfate, sulfite, bisulfite,nitrate, phosphate, monohydrogenphosphate, dihydrogenphosphate,metaphosphate, pyrophosphate, chloride, bromide, iodide, acetate,propionate, caprylate, isobutyrate, oxalate, malonate, succinate,suberate, sebacate, fumarate, maleate, mandelate, benzoate,chlorobenzoate, methylbenzoate, dinitrobenzoate, phthalate,benzenesulfonate, toluenesulfonate, phenylacetate, citrate, lactate,maleate, tartrate, methanesulfonate, and the like. Also contemplated aresalts of amino acids such as arginate and the like and gluconate,galacturonate (see, for example, Berge et al., “Pharmaceutical Salts,”J. of Pharmaceutical Science, 1977, 66, 1-19).

[0071] The acid addition salts of the basic compounds can be prepared bycontacting the free base form with a sufficient amount of the desiredacid to produce the salt in the conventional manner. The free base formcan be regenerated by contacting the salt form with a base and isolatingthe free base in the conventional manner. The free base forms may differfrom their respective salt forms somewhat in certain physical propertiessuch as solubility in polar solvents, but otherwise the salts areequivalent to their respective free base for purposes of the presentinvention.

[0072] Pharmaceutically acceptable base addition salts can be formedwith metal ions or amines, such as alkali and alkaline earth metal ionsor organic amines. Examples of metal ions which are used as cationsinclude sodium, potassium, magnesium, calcium, and the like. Examples ofsuitable arines are N,N′-dibenzylethylenediamine, chloroprocaine,choline, diethanolamine, ethylenediamine, N-methylglucamine, andprocaine (see, for example, Berge et al , “Pharmaceutical Salts,” J. ofPharmaceutical Science, 1977, 66, 1-19).

[0073] The base addition salts of acidic compounds can be prepared bycontacting the free acid form with a sufficient amount of the desiredbase to produce the salt in the conventional manner. The free acid formcan be regenerated by contacting the salt form with an acid andisolating the free acid in the conventional manner. The free acid formsmay differ from their respective salt forms somewhat in certain physicalproperties such as solubility in polar solvents, but otherwise the saltsare equivalent to their respective free acid for purposes of the presentinvention.

[0074] Processes for Preparing the Compounds

[0075] The compounds of the present invention can be prepared by avariety of methods, using procedures well known to those of skill in theart. In one aspect of the present invention, a method for preparingcompounds of Formula I is shown in Scheme 1 below.

[0076] Treatment of a compound of Formula Ia with a primary amine(R³—NH₂) provides a compound of Formula Ib. This reaction isconveniently carried out in a solvent which is inert under the reactionconditions, preferably a halogenated aliphatic hydrocarbon, especiallydichloromethane, an optionally halogenated aromatic hydrocarbon, anopen-chain or cyclic ether (e.g. tetrahydrofuran), a formamide or alower alkanol. Suitably, the reaction is carried out at about −20° C. toabout 120° C.

[0077] Reduction of a compound of Formula Ib provides an alcohol ofFormula Ic. This reduction is typically carried out using lithiumaluminum hydride in a manner well known to those of skill in the art(e.g., in a solvent which is inert under the conditions of thereduction, preferably an open-chain or cyclic ether, especiallytetrahydrofuran, at about −20° C. to about 70° C., preferably at about0° C. to about room temperature).

[0078] Oxidation of an alcohol of Formula Ic in the next step provides acarboxaldehyde of Formula Id. The oxidation is typically carried outwith manganese dioxide, although numerous other methods can also beemployed (see, for example, ADVANCED ORGANIC CHEMISTRY, 4^(TH) ED.,March, John Wiley & Sons, New York (1992)). Depending on the oxidizingagent employed, the reaction is carried out conveniently in a solventwhich is inert under the specific oxidation conditions, preferably ahalogenated aliphatic hydrocarbon, especially dichloromethane, or anoptionally halogenated aromatic hydrocarbon. Suitably, the oxidation iscarried out at about 0° C. to about 60° C.

[0079] Reaction of a carboxaldehyde of Formula Id with an arylsubstituted acetate Ar¹—CH₂—CO₂R (where R is an alkyl group) in apresence of a base provides a compound of Formula Ie. Any relativelynon-nucleophilic base can be used including carbonates, such aspotassium carbonate, lithium carbonate, and sodium carbonate;bicarbonates, such as potassium bicarbonate, lithium bicarbonate, andsodium bicarbonate; amines, such as secondary and tertiary amines; andresin bound amines such as 1,3,4,6,7,8-hexahydro-2Hpyrimido[1,2-a]pyrimidine. To increase the product yield and/or toincrease the reaction rate, water which is formed in the reaction can beremoved by azeotrope. Conveniently, the reaction is carried out in asolvent which is relatively polar but inert under the reactionconditions, preferably an amide such as dimethyl formamide,N-substituted pyrrolidinone, especially 1-methyl-2-pyrrolidinone, and ata temperature of about 70° C. to about 150° C., especially at or nearthe reflux temperature of the solvent to assist in the noted azeotropicremoval of water.

[0080] Oxidation of Ie with an oxidizing agent, such as3-chloroperbenzoic acid (i.e., MCPBA) and Oxone® provides a sulfone (If)which can be converted to a variety of target compounds. Typically theoxidation of Ie is carried out in a solvent which is inert under theconditions of the oxidation. For example, when MCPBA is used as theoxidizing agent, the solvent is preferably a halogenated aliphatichydrocarbon, especially chloroform. When Oxone® is used as the oxidizingagent, the solvent can be water or a mixture of an organic solvent (suchas acetonitrile) and water. The reaction temperature depends on thesolvent used. For an organic solvent, the reaction temperature isgenerally at about −20° C. to about 50° C., preferably about 0° C. toabout room temperature. When water is used as the solvent, the reactiontemperature is generally from about 0° C. to about 50° C., preferablyabout 0° C. to about room temperature. Alternatively, the oxidation canbe carried under catalytic conditions with rhenium/peroxide basedreagents. See, for example, “Oxidation of Sulfoxides by HydrogenPeroxide, Catalyzed by Methyltrioxorhenium(VII)”, Lahti, David W.;Espenson, James H, Inorg. Chem. 2000, 39(10) pp.2164-2167; “Rhenium oxocomplexes in catalytic oxidations,” Catal. Today, 2000, 55(4), pp317-363and “A Simple and Efficient Method for the Preparation of PyridineN-Oxides”, Coperet, Christophe; Adolfsson, Hans; Khuong, Tinh-AlfredoV.; Yudin, Andrei K.; Sharpless, K. Barry, J. Org. Chem., 1998, 63(5),pp1740-1741, which are incorporated herein by reference in theirentirety.

[0081] Reaction of the compound If with an amine (R²—NH₂) provides thecompounds of Formula I′ (i.e. compounds I, wherein R¹ is hydrogen).Further alkylation of I′ then provides compounds of Formula I, where R¹is not hydrogen. The reaction can be carried out in the presence orabsence of solvent. Conveniently, the reaction is carried out attemperatures of from about 0° C. to about 200° C., more preferably aboutroom temperature to about 150° C. Alternatively, in some cases ratherthan using the sulfone If, the sulfide Ie or the corresponding sulfoxidecan be reacted directly an amine (R¹—NH₂) to provide the compounds ofFormula I′. Furthermore, If can also be alkylated with an amine ofR¹R²NH directly to provide a compound of Formula I where R¹ and R2 areas described in the Summary of the Invention.

[0082] Accordingly, the present invention provides a method of preparingcompounds of Formula I, by treating a compound of general Formula Ie orIf with an amine (R¹—NH₂) and optionally reacting the resulting productwith R¹—L, where R¹ is defined above, but excludes hydrogen, and L is aleaving group.

[0083] Alternatively, the carboxaldehyde of the Compound of Formula Iecan be prepared as shown in Scheme II below, which eliminates a need foran ester reduction and an alcohol oxidation in Scheme I.

[0084] Treatment of a compound of Formula II-a (where each R^(a) isindependently alkyl) with an alkyl formate (e.g., methylformate) in thepresence of a base provides a compound of Formula II-b (where M is ametal). This reaction is conveniently carried out at a temperature rangeof from about 0° C. to about 100° C. Typically, an ether, such as THF,and other solvents which are inert to the reaction conditions is used.Suitable bases include alkoxides, such as tert-butoxides, and otherrelatively non-nucleophilic bases that are capable of deprotonating thecompound of Formula II-a.

[0085] Cyclization of a compound of Formula II-b with thiourea in thepresence of a base affords a pyrimidine, of Formula II-c. Typically,this cyclization reaction is conducted in an alcoholic solvent underrefluxing conditions using a corresponding alkoxide as a base.

[0086] Alkylation of a compound of Formula II-c with an alkylating agentR—X¹ (where R is an alkyl group and X¹ is a leaving group, such ashalide) in the presence of a base then provides a compound of FormulaII-d. Suitable bases include a relatively non-nucleophilic basesincluding carbonates, such as potassium carbonate, lithium carbonate,and sodium carbonate; and bicarbonates, such as potassium bicarbonate,lithium bicarbonate, and sodium bicarbonate. Conveniently, the reactionis carried out in a relatively polar solvent that inert under thereaction conditions, preferably acetone, dimethylformamide (DMF) ormethylpyrrolidinone (MP).

[0087] Reaction of a compound of Formula II-d with an aryl substitutedacetate Ar¹—CH₂-CO₂R (where R is an alkyl group) under similarconditions as that described for preparation of a compound of Formula Iein Scheme I above, then provides a compound of Formula II-e. While thealkylation of a compound of Formula II-c is generally conducted prior tothe reaction with an aryl substituted acetate, the order of these tworeactions are not crucial and can be reversed. Thus, a compound ofFormula II-c can be reacted with an aryl substituted acetateAr¹—CH₂—CO₂R and the resulting product can be alkylated with analkylating agent R—X¹ to provide a compound of Formula II-e.

[0088] Alkylation of the amine group of a compound of Formula II-e withan alkylating agent R³—X² (where R³ is those defined above and X² is aleaving group, such as halide) then provides a compound of Ie which canbe further converted to a compound of Formula I′ as described in SchemeI.

[0089] Thus, another aspect of the present invention provides a methodof preparing a pyrimidine compound of Formula II-c by reacting an acetalof the Formula II-a with an alkyl formate and reacting the resultingproduct with a thiourea.

[0090] Yet another aspect of the present invention provides a method forpreparing a compound of Formula II-e, by reacting a compound of FormulaII-c with an alkylating agent or an aryl substituted acetate, andreacting the resulting product with an aryl substituted acetate or analkylating agent, respectively.

[0091] One of skill in the art will understand that certainmodifications to the above schemes are contemplated and within the scopeof the present invention. For example, certain steps will involve theuse of protecting groups for functional groups that are not compatiblewith particular reaction conditions.

[0092] Pharmaceutical Compositions Containing the Compounds

[0093] The compounds of Formula I and the pharmaceutically acceptablesalts of basic compounds of Formula I with acids can be used asmedicaments, e.g., in the form of pharmaceutical preparations. Thepharmaceutical preparations can be administered enterally, e.g., orallyin the form of tablets, coated tablets, dragées, hard and soft gelatinecapsules, solutions, emulsions or suspensions, nasally, e.g., in theform of nasal sprays, or rectally, e.g., in the form of suppositories.However, they may also be administered parenterally, e.g., in the formof injection solutions.

[0094] The compounds of Formula I and their aforementionedpharmaceutically acceptable salts can be processed with pharmaceuticallyinert, organic or inorganic carriers for the production ofpharmaceutical preparations. Lactose, corn starch or derivativesthereof, talc, stearic acid or its salts and the like can be used, forexample, as such carriers for tablets, coated tablets, dragees and hardgelatine capsules. Suitable carriers for soft gelatine capsules are, forexample, vegetable oils, waxes, fats, semi-solid and liquid polyols andthe like; depending on the nature of the active ingredient no carriersare, however, usually required in the case of soft gelatine capsules.Suitable carriers for the production of solutions and syrups are, forexample, water, polyols, sucrose, invert sugar, glucose and the like.Suitable carriers for suppositories are, for example, natural orhardened oils, waxes, fats, semi-liquid or liquid polyols and the like.

[0095] The pharmaceutical preparations can also contain preservatives,solubilizers, stabilizers, wetting agents, emulsifiers, sweeteners,colorants, flavorants, salts for varying the osmotic pressure, buffers,masking agents or antioxidants. They can also contain therapeuticallyvaluable substances other than the compounds of Formula I and theiraforementioned pharmaceutically acceptable salts.

[0096] Medicaments which contain a compound of Formula I or apharmaceutically acceptable salt of a basic compound of Formula I withan acid in association with a compatible pharmaceutical carrier materialare also an object of the present invention, as is a process for theproduction of such medicaments which comprises bringing one or more ofthese compounds or salts and, if desired, one or more othertherapeutically valuable substances into a galenical administration formtogether with a compatible pharmaceutical carrier.

[0097] As mentioned earlier, the compounds of Formula I and theiraforementioned pharmaceutically acceptable salts can be used inaccordance with the invention as therapeutically active substances,especially as antiinflammatory agents or for the prevention of graftrejection following transplant surgery. The dosage can vary within widelimits and will, of course, be fitted to the individual requirements ineach particular case. In general, in the case of administration toadults a convenient daily dosage should be about 0.1 mg/kg to about 100mg/kg, preferably about 0.5 mg/kg to about 5 mg/kg. The daily dosage maybe administered as a single dose or in divided doses and, in addition,the upper dosage limit referred to earlier may be exceeded when this isfound to be indicated.

[0098] Finally, the use of compounds of Formula I and theiraforementioned pharmaceutically acceptable salts for the production ofmedicaments, especially in the treatment or prophylaxis of inflammatory,immunological, oncological, bronchopulmonary, dermatological andcardiovascular disorders, in the treatment of asthma, central nervoussystem disorders or diabetic complications or for the prevention ofgraft rejection following transplant surgery, is also an object of theinvention.

[0099] Methods of Using the Compounds and Compositions

[0100] Compounds of Formula I would be useful for, but not limited to,the treatment of any disorder or disease state in a human, or othermammal, which is exacerbated or caused by excessive or unregulated TNFor p38 kinase production by such mammal. Accordingly, the presentinvention provides a method of treating a cytokine-mediated diseasewhich comprises administering an effective cytokine-interfering amountof a compound of Formula I, or a pharmaceutically acceptable salt ortautomer thereof.

[0101] Compounds of Formula I would be useful for, but not limited to,the treatment of inflammation in a subject, and for use as antipyreticsfor the treatment of fever. Compounds of the invention would be usefulto treat arthritis, including but not limited to, rheumatoid arthritis,spondyloarthropathies, gouty arthritis, osteoarthritis, systemic lupuserythematosus and juvenile arthritis, osteoarthritis, gouty arthritisand other arthritic conditions. Such compounds would be useful for thetreatment of pulmonary disorders or lung inflammation, including adultrespiratory distress syndrome, pulmonary sarcoidosis, asthma, silicosis,and chronic pulmonary inflammatory disease. The compounds are alsouseful for the treatment of viral and bacterial infections, includingsepsis, septic shock, gram negative sepsis, malaria, meningitis,cachexia secondary to infection or malignancy, cachexia secondary toacquired immune deficiency syndrome (AIDS), AIDS, ARC (AIDS relatedcomplex), pneumonia, and herpes virus. The compounds are also useful forthe treatment of bone resorption diseases, such as osteoporosis,endotoxic shock, toxic shock syndrome, reperfusion injury, autoimmunedisease including graft vs. host reaction and allograft rejections,cardiovascular diseases including atherosclerosis, thrombosis,congestive heart failure, and cardiac reperfusion injury, renalreperfusion injury, liver disease and nephritis, and myalgias due toinfection.

[0102] The compounds are also useful for the treatment of Alzheimer'sdisease, influenza, multiple sclerosis, cancer, diabetes, systemic lupuserthrematosis (SLE), skin-related conditions such as psoriasis, eczema,burns, dermatitis, keloid formation, and scar tissue formation.Compounds of the invention also would be useful to treatgastrointestinal conditions such as inflammatory bowel disease, Crohn'sdisease, gastritis, irritable bowel syndrome and ulcerative colitis. Thecompounds would also be useful in the treatment of ophthalmic diseases,such as retinitis, retinopathies, uveitis, ocular photophobia, and ofacute injury to the eye tissue. Compounds of the invention also would beuseful for treatment of angiogenesis, including neoplasia; metastasis;ophthalmological conditions such as corneal graft rejection, ocularneovascularization, retinal neovascularization includingneovascularization following injury or infection, diabetic retinopathy,retrolental fibroplasia and neovascular glaucoma; ulcerative diseasessuch as gastric ulcer; pathological, but non-malignant, conditions suchas hemangiomas, including infantile hemangiomas, angiofibroma of thenasopharynx and avascular necrosis of bone; diabetic nephropathy andcardiomyopathy; and disorders of the female reproductive system such asendometriosis. The compounds of the invention may also be useful forpreventing the production of cyclooxygenase-2.

[0103] Besides being useful for human treatment, these compounds arealso useful for veterinary treatment of companion animals, exoticanimals and farm animals, including mammals, rodents, and the like. Morepreferred animals include horses, dogs, and cats.

[0104] The present compounds may also be used in co-therapies, partiallyor completely, in place of other conventional antiinflammatories, suchas together with steroids, cyclooxygenase-2 inhibitors, NSAIDs, DMARDS,immunosuppressive agents, 5-lipoxygenase inhibitors, LTB₄ antagonistsand LTA₄ hydrolase inhibitors.

[0105] As used herein, the term “TNF mediated disorder” refers to anyand all disorders and disease states in which TNF plays a role, eitherby control of TNF itself, or by TNF causing another monokine to bereleased, such as but not limited to IL-1, IL-6 or IL-8. A disease statein which, for instance, IL-1 is a major component, and whose productionor action, is exacerbated or secreted in response to TNF, wouldtherefore be considered a disorder mediated by TNF.

[0106] As used herein, the term “p38 mediated disorder” refers to anyand all disorders and disease states in which p38 plays a role, eitherby control of p38 itself, or by p38 causing another factor to bereleased, such as but not limited to IL-1, IL-6 or IL-8. A disease statein which, for instance, IL-1 is a major component, and whose productionor action, is exacerbated or secreted in response to p38, wouldtherefore be considered a disorder mediated by p38.

[0107] As TNF-β has close structural homology with TNF-α (also known ascachectin), and since each induces similar biologic responses and bindsto the same cellular receptor, the synthesis of both TNF-α and TNF-β areinhibited by the compounds of the present invention and thus are hereinreferred to collectively as “TNF” unless specifically delineatedotherwise.

EXAMPLES

[0108] Additional objects, advantages, and novel features of thisinvention will become apparent to those skilled in the art uponexamination of the following illustrative examples thereof, which arenot intended to be limiting.

Example 1

[0109]

[0110] This example illustrates the preparation of sulfone 1 from ethyl4-chloro-2-methylthiopyrimidine-5-carboxylate.

[0111] Step 1.1 Preparation of Ethyl4-methylamino-2-methylthiopyrimidine-5-carboxylate

[0112] A solution of 20 g (86 mmol) of ethyl4-chloro-2-methylthiopyrimidine-5-carboxylate (Aldrich Chemical Co.,Milwaukee, Wis., USA) in 250 mL of dichloromethane was cooled to 0° C.and treated slowly with 35 mL (281 mmol) of a 33% solution ofmethylamine in ethanol. After stirring for 30 minutes, 150 mL of waterwas added and the phases were separated. The organic phase was driedover magnesium sulfate and filtered. The filtrate was evaporated underreduced pressure to give 19 g (97%) of ethyl4-methylamino-2-methylthiopyrimidine-5-carboxylate as a white solid.

[0113] Step 1.2 Preparation of4-methylamino-2-methylthiopyrimidine-5-methanol

[0114] Lithium aluminum hydride (9 g, 237 mmol) was stirred in 300 mL ofdry tetrahydrofuran and treated dropwise with a solution of 34 g (143mmol) of ethyl 4-methylamino-2-methylthio-pyrimidine-5-carboxylate in300 mL of dry tetrahydrofuran and left to stand for 15 minutes. Themixture was cooled in ice and cautiously treated dropwise with 18 mL ofwater. Sodium hydroxide solution (36 mL, 2M) was added dropwise,followed by 48 mL of water. The resulting suspension was stirred for 17hours at room temperature and then filtered. The filter residue waswashed twice with 100 mL of ethyl acetate. The filtrate and washingswere combined and evaporated under reduced pressure. The residue wassuspended in 200 mL of dichloromethane/hexane (2:1) and the solid wasfiltered and dried to give 23.5 g (86%) of4-methylamino-2-methylthiopyrimidine-5-methanol as a yellow solid.

[0115] Step 1.3 Preparation of4-methylamino-2-methylthiopyrimidine-5-carboxaldehyde

[0116] 4-Methylamino-2-methylthiopyrimidine-5-methanol (20 g, 108 mmol)and 1 L of dichloromethane were combined with stirring and treated with87 g (1 mol) of manganese dioxide. The resulting suspension was stirredfor 24 hours and then filtered through a filter aid. The filter residuewas washed with 100 mL of dichloromethane and the combined filtrate andwashings were evaporated under reduced pressure to give 15.8 g (80%) of4-methylamino-2-methylthiopyrimidine-5-carboxaldehyde as a white solid.

[0117] Step 1.4

[0118] To a mixture of 3.3 g (18.1 mmol) of4-methylamino-2-methylthiopyrimidine-5-carboxaldehyde, 4.0 g (20.1 mmol)of ethyl-2-chlorophenylacetate in 30 mL of NMP was added 1.5 g of resin,polymer bound 1,3,4,6,7,8-hexahydro-2H pyrimido[1,2-a]pyrimidine. Thereaction mixture was heated to 120° C. After 48 h, the reaction mixturewas cooled to room temperature and filtered. The resin was washed withNMP and ethyl acetate. The filtrate was diluted with water and filtered.The product was isolated by filtration and by extraction of the filtratewith ethyl acetate. The product was washed with 5% aqueous HCl and waterand dried to give 4.0 g of sulfide (mass spec. MH+=318. Mpt.193.0-193.4).

[0119] Step 1.5

[0120] A solution of 13.5 g (42.5 mmol) of sulfide in chloroform wascooled in ice and treated with 20.5 g (91 mmol) of 3-chloroperbenzoicacid. The mixture was stirred at room temperature for 16 hours anddiluted with saturated aqueous sodium bicarbonate solution. The phaseswere separated. The organic phase was dried over magnesium sulfate andfiltered. The filtrate was concentrated under reduced pressure and theproduct was stirred in ethyl ether, filtered and dried to give 13.1 g ofsulfone 1 (mass spec. MH+=350. Mpt. 232.6-232.8).

Example 2

[0121]

[0122] This example illustrates the preparation of6-(2-chlorophenyl)-2-methanesulfonyl-pyrido[2,3-d]pyrimidin-7-olstarting with ethyl 4-chloro-2-methylthiopyrimidine-5-carboxylate.

[0123] Step 2.1 Preparation of ethyl4-amino-2-methylthiopyrimidine-5-carboxylate

[0124] A solution of ethyl 4-chloro-2-methylthiopyrimidine-5-carboxylate(25.4 g, 106 mmol, Aldrich Chemical Co., Milwaukee, Wis., USA) in 300 mLof tetrahydrofuran was treated with 50 mL of triethylamine and 40 mL ofaqueous ammonium hydroxide. After stirring for 4 hours, 300 mL of waterwas added and the phases were separated. The organic layer was washedwith 300 mL of brine, concentrated in vacuo, dissolved in methylenechloride, dried over sodium sulfate, filtered and concentrated in vacuoto give 16.5 g (95%) of ethyl4-amino-2-methylthiopyrimidine-5-carboxylate as a white solid. Step 2.2Preparation of 4-amino-2-methylthiopyrimidine-5-methanol

[0125] To a 0° C. solution of lithium aluminum hydride (175 niL, 175mmol) in diethyl ether was added dropwise a solution of4-amino-2-methylthiopyrimidine-5-carboxylate (34.7 g, 163 mmol) in 500mL of dry tetrahydrofuran over a period of 1.5 hours. The reactionmixture was slowly warmed to ambient temperature and then cooled back to0 ° C. before carefully quenching with 7 mL of water, 7 mL of 2 M sodiumhydroxide solution, followed by 14 mL of water. The resulting suspensionwas filtered and the residue was washed with 2×300 mL of ethyl acetate.The filtrates were combined and concentrated to give 23.0 g (83%) of4-amino-2-methylthiopyrimidine-5-methanol as a white solid.

[0126] Step 2.3 Preparation of4-amino-2-methylthiopyrimidine-5-carboxaldehyde

[0127] A suspension of 4-amino-2-methylthiopyrimidine-5-methanol (21.8g, 128 mmol) in 800 mL of methylene chloride was treated with activatedmanganese oxide powder (63.0 g, 725 mmol). The reaction mixture wasstirred for 18 hours, then filtered through a pad of celite. The solidresidue was repeatedly washed with a solution of hot methylene chlorideand methanol. The filtrates were combined and concentrated to give 17.5g (81%) of 4-amino-2-methylthiopyrimidine-5-carboxaldehyde as a whitesolid.

[0128] Step 2.4 Preparation of6-(2-chlorophenyl)-2-methylthio-pyrido[2,3-d]pyrimidin-7-ol

[0129] To a solution of 4-amino-2-methylthiopyrimidine-5-carboxaldehyde(21.7 g, 128 mmol) and ethyl-2-chlorophenylacetate (31.3 g, 158 mmol) in250 mL of dry 1-methyl -2-pyrrolidinone was added potassium carbonate(63.0 g, 491 mmol). The reaction mixture was stirred at 95° C. for 16hours and monitored by TLC (20:80, ethyl acetate/hexanes). An additional12.0 g (60 mmol) of ethyl-2-chlorophenylacetate was added and thereaction mixture was stirred at 95° C. for another 16 hours. Thereaction mixture was cooled and filtered. The filtered solids werewashed with ethyl acetate. The filtrates were combined and diluted with400 mL of water and 300 mL of ethyl acetate. The phases were separated,and the organic layer was washed with brine, dried over sodium sulfate,filtered and concentrated in vacuo until a yellow precipitate formed.The solids were washed with ethyl acetate and dried to yield a minoramount of product. Most of the product remained in the aqueous layer andslowly precipitated out upon standing. The resulting suspension thatformed was filtered and washed with water and ethyl acetate. Thisprocedure was repeated six times yielding a total of 31.9 g (82%) of6-(2-chlorophenyl)-2-methanesulfonyl-pyrido[2,3-d]pyrimidin-7-ol. Massspec. M⁺=303, mp=234.5-235.3° C.

[0130] Step 2.5 Preparation of6-(2-chlorophenyl)-2-methanesulfonyl-pyrido[2,3-d]pyrimidin-7-ol

[0131] To a solution of6-(2-chlorophenyl)-2-methylthio-pyrido[2,3-d]pyrimidin-7-ol (25.2 g,82.9 mmol) was added a slurry of Oxone™ (105 g, 171 mmol) in 200 mL ofwater. The reaction mixture was stirred for 5 hours, filtered andconcentrated in vacuo. The resulting slurry was filtered and thecollected solids were successively washed with water four times anddried to give 23.2 g (83%) of6-(2-chlorophenyl)-2-methanesulfonyl-pyrido[2,3-d]pyrimidin-7-ol as alight-yellow solid. Mass spec. MH⁺=336, mp=215.1-221.1 ° C.

Example 3

[0132] This example illustrates the preparation of6-(2-chlorophenyl)-2-[(1-methyl-piperidin-4-ylmethyl)-amino]-8H-pyrido[2,3-d]pyrimidin-7-one.

[0133] The sulfone 2 (0.5 g, 1.49 mmol) was combined with1-methyl-4-aminomethylpiperidine (0.57 g, 4.47 mmol). The mixture washeated to 110° C. and stirred for 2 hours. The reaction was cooled toroom temperature and the residue was dissolved inmethanol/dichloromethane, and purified by column chromatography onsilica gel in 10% methanol/dichloromethane. The fractions containing theproduct was combined and concentrated. The resulting residue wasdissolved in 15 ml of 10% methanol/dichloromethane and treated with 1equivalent of 1M HCI in ether. The solution was concentrated to aresidue and triturated in ether. The solid was filtered and dried toyield 0.25 g of6-(2-chlorophenyl)-2-[(1-methyl-piperidin4-ylmethyl)-amino]-8H-pyrido[2,3-d]pyrimidin-7-one,HCl salt. Mass spec. MH⁺=383, melting pt.=213-220° C.

Example 4

[0134]

[0135] Step 4.1 Preparation of 4B

[0136] To a solution of compound 4A (4.704 g, 18.94 mmol) in DMF (30 mL)was added sodium carbonate (2.2 g, 1.1 eq) followed by2-chloro-N,N-dimethyl acetamide (2.14 mL, 1.1 eq). The resulting mixturewas stirred vigorously at room temperature for 18 hours. TLC indicatedthat more than 50% starting material remained so the reaction was heatedto 80° C. for an additional 24 hours. Once again, TLC analysis showedthat there was a substantial amount of starting material remaining, sothe mixture was cooled to room temperature and then additional2-chloro-N,N-dimethyl acetamide (0.58 mL, 0.3 eq) was added. Thereaction was heated to 80° C. for another 4.5 hours whereby analysis byTLC indicated that there was very little starting material remaining.Then, ethyl acetate (150 mL) and water (50 mL) were added, and themixture was partitioned and the layers were separated. The aqueous layerwas further extracted with ethyl acetate (1×50 mL) and the combinedorganic layers were washed with brine (3×35 mL). The organic layers werecombined, dried over magnesium sulfate, filtered and concentrated anddried under vacuum to give 9.9 g of crude product. Purification by flashchromatography using silica gel and gradient elution (neatdichloromethane to 10% methanol in dichloromethane) afforded compound 4B(3.91 g) as a thick syrup. MH⁺=334.

[0137] Step 4.2 Preparation of 4C

[0138] The compound 4B was taken up in ethanol (120 mL) and nitrogen gaswas gently bubbled over the solution for 5 minutes. Then 10% palladiumon activated charcoal (1.5 g) was added and the mixture was placed under1 atmosphere of hydrogen gas and stirred at room temperature for 18hours. Analysis by TLC indicated that the reaction was complete so themixture was filtered through a 2.5 cm bed of celite. The filtrate wasconcentrated and dried under vacuum to afford the compound 4C,4-aminomethyl-1-dimethylaminocarbonylmethyl-piperidine (2.15 g) as anoil. (M+H)⁺=200.

[0139] Step 4.3 Preparation of 4

[0140] The sulfone 2 (200 mg, 0.614 mmol), the compound 4C (367 mg, 3eq) and N-methyl pyrolidinone (0.3 mL) were mixed in a 10 mL flask andheated at 110° C. with stirring. After 5 minutes, the fluid mixtureturned to a solid and by TLC analysis the reaction was complete. Thereaction mixture was cooled and methanol (20 mL) was added. Theprecipitate was crushed up and then filtered to yield a white powder(235 mg). M.p.=263.1-263.5° C., (M+H)⁺455. This free amine (230 mg) wasdissolved in dichloromethane (50 mL) and methanol (50 mL) and HCl gaswas bubbled through the solution for 15 minutes. The vessel was cappedtightly and stirred for 2 hours. Then the solvent was removed underreduced pressure at 50° C. and coevaporated with dichloromethane twotimes. The resulting HCl salt was dried under vacuum at 56° C. for 8hours to give the compound 4 (276 mg) as an off-white solid.M.p.=211.8-212.8° C., (M+H)⁺=455 (free base).

Example 5

[0141]

[0142] Step 5.1 Preparation of 5A

[0143] The compound 4A (4.632 g, 18.65 mmol) was dissolved indimethylformamide (30 mL). To this solution was added sodium carbonate(2.17 g, 1.1 eq) and t-butyl bromoacetate (3 mL, 1.1 eq). The resultingmixture was stirred vigorously at room temperature for 18 hours. TLCanalysis showed that very little starting material was present. Ethylacetate (100 mL) and water (100 mL) were added to the reaction, and themixture was partitioned and the layers were separated. The aqueous layerwas further extracted with ethyl acetate (2×100 mL). The organic layerswere combined, washed with water (1×75 mL) and brine (1×75 mL), driedover magnesium sulfate, filtered, concentrated and dried under vacuum togive 6.5 g of the crude product. Purification by flash columnchromatography on silica gel using 3% methanol in dichloromethane as theeluent gave 5A (3.95 g) as a thick syrup, (M+H)⁺=363.

[0144] Step 5.2 Preparation of 5B

[0145] The compound 5A (3.95 g, 10.9 mmol) was dissolved in ethanol (125mL) and nitrogen gas was gently passed over the mixture for 5. minutes,then 10% palladium on activated charcoal (1.5 g) was added. Theresulting mixture was placed under 1 atmosphere of hydrogen gas andstirred for 18 hours. TLC analysis-indicated that the reaction wascomplete and the reaction was filtered through a 2.5 cm bed of celite.The filtrate was concentrated and dried under vacuum to afford thecompound 5B, 4-aminomethyl-1-tert -butyloxycarbonylmethyl-piperidine asa colorless oil (2.26 g). (M+H)⁺=229.

[0146] Step 5.3 Preparation of compound 5

[0147] The sulfone 2 (200 mg, 0.614 mmol), compound 5B (420 mg, 3 eq),and N-methyl pyrrolidinone were mixed in a 10 mL flask and heated to110° C. with stirring. The fluid mixture became semi-solid after about10 minutes. The mixture was stirred for another 20 minutes and TLCanalysis showed that the reaction was complete. Then 15 mL of ethylacetate and 100 mL hexanes were added to the reaction mixture. Theprecipitated product was crushed up and filtered to provide a whitepowder. The powder was washed with 60 mL of hexanes and vacuum dried toyield 270 mg of the free amine t-butyl ester as a white powder.M.p.=217.6-220.0° C., (M+H)⁺=484. The free amine was dissolved indioxane (100 mL) and HCl gas was bubbled through the solution for 15minutes resulting in a homogeneous solution. The vessel was cappedtightly and stirred at room temperature for 18 hours. The resultingprecipitate was filtered and dried at 56° C. for 8 hours to give the HClsalt 11 (200 mg). M.p.=235.3-237.9° C., (M+H)⁺=428 (free aminecarboxylic acid).

Example 6

[0148]

[0149] Step 6.1 Preparation of 6A

[0150] The compound 4A (4.889 g, 19.69 mmol) was dissolved indimethylformamide (30 mL) and sodium carbonate (2.3 g, 1.1 eq) was addedfollowed by 2-bromoacetamide (2.99 g, 1.1 eq) and the resulting mixturewas stirred vigorously at room temperature for 18 hours. Analysis by TLCshowed that the reaction was nearly complete. Ethyl acetate (150 mL) andwater (50 mL) were added, and the mixture was partitioned and the layerswere separated. The organic layer was washed with water (2×50 mL) andbrine (1×75 mL), dried over magnesium sulfate, filtered, concentratedand vacuum dried to provide a solid. Hexanes (300 mL) were added to theresidue and the solids were crushed up and mixed well. The supernatantwas then decanted. This procedure was repeated again with 300 mL ofhexanes. The residue was dried under vacuum to give a white powder 6A(3.13 g). (M+H)⁺=306.

[0151] Step 6.2 Preparation of 6B

[0152] The compound 6A (3.1 g, 10.2 mmol) was dissolved in ethanol (250mL) and nitrogen gas was gently bubbled through the mixture for 5minutes. A mixture of 10% palladium on activated carbon (1.45 g) wasadded. The resulting mixture was placed under 1 atmosphere of hydrogenand stirred for 18 hours. The mixture was filtered through a 2.5 cm bedof celite. The filtrate was concentrated under reduced pressure at 40°C. and dried under vacuum to give the compound 6B (1.77g) as a stickywhite solid. (M+H)⁺=172.

[0153] Step 6.3 Preparation of the compound 6

[0154] The sulfone 2 (400 mg, 1.23 mmol), the compound 6B (630 mg, 3 eq)and N-methyl pyrolidinone (0.3 mL) were mixed in a 25 mL flask and themixture was heated to 110° C. with stirring for 30 minutes. The fluidmixture became a solid and TLC analysis indicated that the reaction wascomplete. The reaction mixture was diluted with about 20 mL of methanoland the white solid was filtered and dried to give 410 mg of the freeamine primary amide. M.p.=244.6-245.9° C., (M+H)⁺=427. This free amineprimary amide was then dissolved in methanol (100 mL) and HCl gas wasbubbled through the solution for 10 minutes. The vessel was then cappedtightly and stirred at room temperature for 3 days. The solvent wasremoved under reduced pressure at 40° C. and then 10 mL of methanol wasadded to the residue. To the resulting solution was addedtetrahydrofuran (100 mL) and the precipitate that was formed wasfiltered and collected to give the compound 6 as an off-white powder(250 mg). M.p.=220.0-221.1° C., (M+H)⁺=442 (free amine, methyl ester).

Example 7

[0155]

[0156] To a solution of the compound 9B (0.28 g, 2 mmol) in acetonitrile(5 mL) at room temperature was added TMSCN (0.8 mL, 3 eq). The resultingmixture was heated to 80° C. with stirring until the mixture washomogeneous. Then, sulfone 1 (0.35 g, 1 mmol) was added and the reactionwas stirred at 80° C. for 40 minutes. The reaction was quenched withmethanol (10 mL) and stirred for 5 minutes. After concentrating underreduced pressure at 50° C., ethyl acetate (35 mL) and water (25 mL) wereadded to the residue. The organic layer was separated, washed with water(2×25 mL) and brine (1×25mL), dried over magnesium sulfate, filtered,concentrated and dried to give 408 mg of crude material. Purification bypreparative thin layer chromatography afforded the amine as an off-whitepowder (299 mg). (M+H)⁺=373, M.P.=91.4-93.2° C. The free amine wasdissolved in ethyl acetate (10 mL) and with stirring at room temperaturewas added a solution of 1M HCl in diethyl ether (1.2 mL, 1.5 eq). Afterstirring for 30 minutes, the solvent was removed under reduced pressureat 55° C. Further concentration under high vacuum at 56° C. for 6 hoursgave compound 7 as an off-white powder (275 mg). (M+H)⁺=373,M.P.=178.0-181.5° C.

Example 8

[0157] This example illustrates the preparation of6-(2-chlorophenyl)-2-[(1,1-dimethyl-2-hydroxyethyl)amino]-8H-pyrido[2,3-d]pyrimidin-7-one.

[0158] A mixture of 0.350 g (1.0 mmol) of sulfone 1 and 0.445 g (5.0mmol) was stirred at 120° C. for 1 hour and then cooled to roomtemperature. The crude product was purified by column chromatography (5%methanol/dichloromethane) to give the desired product as a foam. Theresidue was suspended in methanol and addition of hydrochloric acid (1.0M/Et₂O, 1 equivalent), stirred for 20 minutes and concentrated underreduced pressure. The residue was stirred in a mixture of MeOH/Et₂O for1 hour, and the product was filtered to provide a white solid. Yield 190mg. Mpt. 228.6-228.9° C. (HCl salt).

Example 9

[0159]

[0160] To a solution of compound 9B (Chem. Pharm. Bull. 45, 1997,185-188) (0.28 g, 2 mmol) in acetonitrile (4 mL) at room temperature wasadded TMSCN (0.8 mL, 3 eq). The resulting mixture was heated to 80° C.until the mixture became homogeneous. Then 9A (0.4 g, 1 mmol) was addedto the reaction mixture and stirred at 80° C. for 35 minutes. Thereaction mixture was cooled to room temperature and 15mL of methanol wasadded and stirred for 5 minutes. The reaction mixture was concentratedunder reduced pressure at 50 ° C. The residue was diluted with ethylacetate (35 mL) and water (25 mL). The organic phase was separated,washed with water (1×25 mL) and brine (1×25 mL), dried over magnesiumsulfate, filtered and concentrated to yield 445 mg of crude material.Purification by preparative thin layer chromatography eluting with 50%ethyl acetate in hexanes gave the free amine as an off-white powder (242mg). (M+H)⁺=453, M.P.=204.7-206.0° C. The free amine was dissolved inethyl acetate (15 mL) at room temperature and a solution of 1M HCl indiethyl ether (0.6 mL, 1.5 eq) was added. The resulting mixture wasstirred for 2 hours. The solvent was removed under reduced pressure at50° C. and the resulting solid was dried under vacuum at 56° C. to givecompound 9 as an off-white powder (219 mg). (M+H)⁺=453,M.P.=142.0-149.0° C.

Example 10

[0161]

[0162] A mixture of sulfone 1 (250 mg, 0.71 mmol) and2-amino-2-methyl-1,3-propanediol (150 mg, 1.4 mmol) in1-methyl-2-pyrrolidinone (0.25 mL) was stirred at 80° C. for 12 h andthen cooled to room temperature. Water (1 mL) was added and thesuspension was stirred for 30 min, filtered and the precipitate waswashed with water, dried and suspended in methanol. The suspension wasagain filtered and dried to give 83 mg of the desired product 10. Mass.spec. MH⁺=374, mpt. 200-210.

Example 11

[0163]

[0164] A mixture of sulfone 1 (250 mg, 0.71 mmol) and2-amino-2-ethyl-1,3-propanediol (170 mg, 1.4 mmol) in1-methyl-2-pyrrolidinone (0.25 niL) was stirred at 80° C. for 12 h andthen cooled to room temperature. Water (1 mL) was added, and thesuspension was stirred for 30 min, filtered and the precipitate waswashed with water, dried and suspended in methanol. The suspension wasagain filtered and dried to give 83 mg of the desired product 11. Massspec. MH⁺=388, mpt. 98.1-102.

Example 12

[0165]

[0166] A mixture of sulfone 1 (250 mg, 0.71 mmol) and(S)-(+)-2-amino-3-methyl -butanol (147 mg, 1.4 mmol) in1-methyl-2-pyrrolidinone (0.25 mL) was stirred at 80° C. for 12 h andthen cooled to room temperature. Water (1 mL) was added, and thesuspension was stirred for 30 min, filtered and the precipitate waswashed with water, dried and suspended in methanol. The suspension wasagain filtered and dried to give 90 mg of the desired product 12. Massspec. MH⁺=372, mpt. 167.1-169.1.

Example 13

[0167]

[0168] A mixture of sulfone 1 (250 mg, 0.71 mmol) and(S)-(+)-2-amino-1-butanol (127 mg, 1.4 mmol) in 1-methyl-2-pyrrolidinone(0.25 mL) was stirred at 80° C. for 12 h and then cooled to roomtemperature. Water (1 mL) was added, and the suspension was stirred for30 min, filtered and the precipitate was washed with water, dried andsuspended in methanol. The suspension was again filtered and dried togive 105 mg of the desired product 13. Mass spec. MH⁺=358, mpt.170.5-172.1.

Example 14

[0169]

[0170] A mixture of sulfone 1 (250 mg, 0.71 mmol) and (S)-tert-leucinol(167 mg, 1.4 mmol) in 1-methyl-2-pyrrolidinone (0.25 mL) was stirred at80° C. for 12 h and then cooled to room temperature. Water (1 mL) wasadded, and the suspension was stirred for 30 min, filtered and theprecipitate was washed with water, dried and suspended in methanol. Thesuspension was again filtered and dried to give 116 mg of the desiredproduct 14. Mass spec. MH⁺=386, mpt. 171.2-174.0.

Example 15

[0171]

[0172] A mixture of sulfone 1 (250 mg, 0.71 mmol) and (R)-(−)-leucinol(167 mg, 1.4 mmol) in 1-methyl-2-pyrrolidinone (0.25 mL) was stirred at80° C. for 12 h and then cooled to room temperature. Water (1 mL) wasadded, and the suspension was stirred for 30 min, filtered and theprecipitate was washed with water, dried and suspended in methanol. Thesuspension was again filtered and dried to give 178 mg of the desiredproduct 15. Mass spec. MH⁺=386, mpt.173.1-176.2.

Example 16

[0173]

[0174] A mixture of sulfone 1 (250 mg, 0.71 mmol) and(S)-(+)-2-amino-1-propanol (107 mg, 1.4 mmol) in1-methyl-2-pyrrolidinone (0.25 niL) was stirred at 80° C. for 12 h atand then cooled to room temperature. Water (1 mL) was added, and thesuspension was stirred for 30 min, filtered and the precipitate waswashed with water, dried and suspended in methanol. The suspension wasagain filtered and dried to give 87 mg of the desired product 16. Massspec. MH⁺=344, mpt.131.1-132.2.

Example 17

[0175]

[0176] A mixture of sulfone 1 (250 mg, 0.71 mmol) and(S)-(+)-isoleucinol (167 mg, 1.4 mmol) in 1-methyl-2-pyrrolidinone (0.25mL) was stirred at 80° C. for 12 h and then cooled to room temperature.Water (1 mL) was added, and the suspension was stirred for 30 min,filtered and the precipitate was washed with water, dried and suspendedin methanol. The suspension was again filtered and dried to give 200 mgof the desired product 17. Mass spec. MH⁺=386, mpt.140.1-143.6.

Example 18

[0177]

[0178] A mixture of sulfone 1 (250 mg, 0.71 mmol) and serinol (130 mg,1.4 mmol) in 1-methyl-2-pyrrolidinone (0.25 mL) was stirred at 80° C.for 12 h and then cooled to room temperature. Water (1 mL) was added,and the suspension was stirred for 30 min, filtered and the precipitatewas washed with water, dried and suspended in methanol. The suspensionwas again filtered and dried to give 179 mg of the desired product 18.Mass spec. MH⁺=360, mpt.155.8-157.3.

Example 19

[0179]

[0180] Step A: Preparation of 4-ethylsulanyl-butan-2-one:

[0181] To a solution mixture of ethanethiol (6.2 g, 7.4 mL, 0.1 mol), 3drops of DBU in 50 mL of THF at 5° C. was added dropwise the methylvinyl ketone (7.3 g, 8.45 mL, 0.105 mol). The solution mixture wasallowed to stir overnight at ambient temperature. The mixture was thenconcentrated in vacuo to afford 13.6 g of the desired ketone.

[0182] Step B: Preparation of 4-ethylsulfanyl-butan-2-one oxime:

[0183] A mixture of the 4-ethylsulfanyl-butan-2-one (13.6 g, 0.1 mol),sodium acetate trihydrate (68 g, 0.5 mol) and hydroxylaminehydrochloride (34.7 g, 0.5 mol) in 500 mL of ethanol was heated torefluxed for 3 hours. The mixture was cooled and concentrated in vacuo.The residue was diluted with water and extracted with ethyl acetate(2×200 mL). The organic solution was then washed with Brine, dried,filtered and concentrated in vacuo to afford 14.7 g of the oxime.

[0184] Step C: Preparation of 2-amino-4-ethylsulfanyl-butane:

[0185] To a solution of lithium aluminum hydride ((1M, 120 mL, 0.12 mol)in tetrahydrofuran at room temperature under a nitrogen atmosphere wasadded dropwise the 4-ethylsulfanyl-butan-2-one oxime (6 g, 0.04 mol) in30 niL of tetrahydrofuran. After addition was completed, the mixture wasstirred at reflux for 4 hours. The suspension was cooled with anice-water bath and water (4.6 mL) in 20 mnL of tetrahydrofuran was addedslowly (dropwise), followed by an aqueous solution of sodium hydroxide(15%, 4.6 mL). Additional water (13.8 mL) was then added and thereaction mixture was stirred for 30 minutes, filtered through a celitepad and rinsed with ethyl acetate (300 mL). The filtrate was dried(brine, MgSO₄) and evaporated under reduced pressure affording 3.43 g ofthe 2-amino-4-ethylsulfanyl-butane (mass spec. M+1=134).

[0186] Step D: Preparation of 19A and 19B:

[0187] A solution of the sulfone 1(0.55 g, 1.6 mmol) and2-amino-4-ethylsulfanyl -butane (0.63 g, 4.8 mmol) in 10 mL oftetrahydrofuran was refluxed for 1 hour. The solution was cooled andconcentrated in vacuo and the product was purified by columnchromatography with silica eluting with 5% ethyl acetate indichloromethane affording 421 mg of a racemic mixture of 19A (mass spec.M+1=403) and 31 mg of the aziridine compound 19B (mass spec. M+1=401,MP=160-167° C.).

Example 20

[0188] This example illustrates an alternative method for producing6-(2-chlorophenyl)-8-methyl-2-methylthio-8-hydropyridino[2,3-d]pyrimidin-7-one(VI)

[0189] Preparation of 3,3-Diethoxy-2-formylpropionitrile Potassium Salt(II)

[0190] To a stirred solution of 3,3-diethoxypropane-nitrile (I, 283.80g, 1.98 moles) and methyl formate (148.80 g, 2.48 moles) in anhydrousTHF (1.1 L) at 10° C. was added 1.0 M potassium tert-butoxide in THF(2.2 L, 2.2 moles). Temperature was maintained in the range of 10° C. to15° C. throughout the 45 minute addition. Following the addition, theresulting slurry was stirred 2 hours at ambient room temperature. Hexane(400 mL) was then added and stirring was continued for another 20 min.The slurry was filtered and the cake washed with 1/1 hexanes/THF anddried overnight at 60° C. in a vacuum oven. The yield of pale tan powderwas 302.5 grams (73.0%). ¹H-NMR (CD₃OD) was consistent with the desiredstructure II.

[0191] Preparation of 4-Amino-2-sulfanylpyrimidine-5-carbaldehyde (III)

[0192] A slurry of thiourea (92.8 g, 1.22 moles) in ethanol (90 mL) washeated under reflux and vigorously stirred. To this slurry was added asuspension of 3,3-diethoxy-2-formylpropionitrile potassium salt II(222.20 g, 1.06 moles) in 25% sodium methoxide/methanol (85.5 mL, 0.37mole) and ethanol (285 mL) in five aliquots over a 10 minute periodwhile maintaining reflux conditions (alternatively, the latter slurrymay be heated to 50° C. to give a homogenous solution for the addition).An additional portion of ethanol (150 mL) was added to facilitatestirring. The thick slurry became a bright yellow color following theaddition and was held under reflux for an additional 1 hour. The mixturewas then cooled and evaporated to near dryness on a rotoevaporator. Theresidue was dissolved in water (940 mL). Crude product was precipitatedfrom solution by the addition of 30% acetic acid (280 mL) and isolatedvia filtration using a medium frit sintered glass filtration funnel. Thecake was washed with water (800 mL). Purification via trituration in hotwater (1 L) for 30 minutes, followed by cooling and-filtration gave118.9 grams (72.3%) of product as a bright yellow solid after dryingovernight at 60° C. in a vacuum oven (subsequent preparations havedemonstrated that this trituration is unnecessary). An HPLC gave purityas 98.67%. ¹H-NMR (DMSO-d6) was consistent with desired structure III.

[0193] Preparation of 4-Amino-2-methylthiopyrimidine-5-carbaldehyde (IV)

[0194] To a solution of 4-amino-2-sulfanyl-pyrimidine-5-carbaldehyde III(100.00 g, 644.4 mmoles) and 325 mesh potassium carbonate (178.10 g,1.29 moles) in acetone (1.5 L) was added iodomethane (128.10 g, 902.2mmoles) dropwise over 20 minutes with mild cooling. The mixture wasstirred at ambient room temperature over the weekend. TLC showedremaining III and an additional aliquot of iodomethane was added (8 mL)and stirring was continued overnight. TLC again showed some IIIremaining and an addition portion of iodomethane was added (8 mL) andstirring was continued another 24 hour period. An HPLC showed 95.9%S-alkylated product and 3.7% of compound III. The reaction mixture wasstripped to near dryness on a rotoevaporator. Water (1 L) was added tothe residue and the product was collected via filtration and washed withwater (200 mL). The product was dried overnight in a vacuum oven at 60°C. Yield was 103.37 grams (94.8%). An HPLC showed 95.8% IV and 4.2% III.

[0195] Preparation of6-(2-chlorophenyl)-2-methylthio-8-hydropyridino[2,3-d]pyrimidin-7-one(V)

[0196] A mixture of IV (10.00 g, 59.1 mmoles), ethyl2-(2-chlorophenyl)acetate (14.40 g, 71.8 mmoles), NMP (115 mL) and 325mesh potassium carbonate (29.00 g, 209.8 mmoles) was heated at 95° C.overnight. The reaction mixture was cooled and diluted with water (800mL). The resulting slurry was stirred overnight and filtered to isolateproduct (V). The filter cake was washed with water and dried at 60° C.in a vacuum oven overnight. Isolated yield was 14.9 grams (83.0%) ofdark tan solid. Analysis by an HPLC showed 98.3% purity.

[0197] Preparation of6-(2-Chlorophenyl)-8-methyl-2-methylthio-8-hydropyridino[2,3-d]pyrimidin -7-one (VI)

[0198] A mixture of V (0.25 g, 0.82 mmole), NMP (5 mL), potassiumcarbonate (0.11 g, 0.82 mmole), and iodomethane (0.14 g, 0.96 mmole) wasstirred under nitrogen at ambient room temperature overnight. Water (15mL) was added and stirring was continued for 24 hours. The slurry wasfiltered and the filter cake washed with water (10 mL). An HPLC showed97.8% purity.

Example 21

[0199] This example illustrate an assay protocol for determining invitro inhibition of p-38 (MAP) Kinase.

[0200] The p-38 MAP kinase inhibitory activity of compounds of thisinvention in vitro was determined by measuring the transfer of theγ-phosphate from γ-³³P-ATP by p-38 kinase to Myelin Basic Protein (MBP),using the a minor modification of the method described in Ahn, N. G.; etal. J. Biol Chem. Vol.266(7), 4220-4227, (1991).

[0201] The phosphorylated form of the recombinant p38 MAP kinase wasexpressed with SEK-1 and MEKK in E. Coli and then purified by affinitychromatography using a Nickel column.

[0202] The phosphorylated p38 MAP Itinase was diluted in kinase buffer(20 mM 3-(N-morpholino)propanesulfonic acid, pH 7.2, 25 mM γ-glycerolphosphate, 5 mM ethylene glycol-bis(beta-aminoethylether)-N,N,N′,N′-tetraacetic acid, 1mM sodium vanadate, 1 mMdithiothreitol, 40 mM magnesium chloride). Test compound dissolved inDMSO or only DMSO (control) was added and the samples were incubated for10 min at 30° C. The kinase reaction was initiated by the addition of asubstrate cocktail containing MBP and γ-³³P-ATP. After incubating for anadditional 20 min at 30° C., the reaction was terminated by adding 0.75%phosphoric acid. The phosphorylated MBP was then separated from theresidual γ-³³P-ATP using a phosphocellulose membrane (Millipore,Bedford, Mass.) and quantitated using a scintillation counter (Packard,Meriden, Conn.).

[0203] Compounds of the invention were active in this assay. The p-38inhibitory. activities (expressed as IC₅₀, the concentration causing 50%inhibition of the p-38 enzyme being assayed) of some compounds of theinvention are: CPD # (from Table 1) IC₅₀, μM 1 0.052 3 2.196 4 6.266 70.0003 8 0.031 10 0.042 11 0.024 12 0.124 13 0.048 18 0.092

Example 22

[0204] This example illustrates an in vitro assay to evaluate theinhibition of LPS-induced TNF-α production in THP1 cells.

[0205] The ability of the compounds of this invention to inhibit theTNF-α release was determined using a minor modificaiton of the methodsdescribed in Blifeld, et al. Transplantation 51:498-503 (1991).

[0206] (a) Induction of TNF Biosynthesis:

[0207] THP-1 cells were suspended in culture medium [RPMI (Gibco-BRL,Gailthersberg, Md.) containing 15% fetal bovine serum, 0.02 mM2-mercaptoethanol], at a concentration of 2.5×10⁶ and then plated in 96well plate (0.2 mL aliquots in each well). Test compounds were dissolvedin DMSO and then diluted with the culture medium such that the finalDMSO concentration was 5%. Twenty five μL aliquots of test solution oronly medium with DMSO (control) were added to each well. The cells wereincubated for 30 min., at 37° C. LPS (Sigma, St. Louis, Mo.) was addedto the wells at a final concentration of 0.5 μg/ml, and cells wereincubated for an additional 2 h. At the end of the incubation period,culture supernatants were collected and the amount of TNF-α present wasdetermined using an ELISA assay as described below.

[0208] (b) ELISA Assay:

[0209] The amount of human TNF-α present was determined by a specifictrapping ELISA assay using two anti-TNF-α antibodies (2TNF-H12 and2TNF-H34) described in Reimund, J. M., et al. GUT. vol. 39(5), 684-689(1996).

[0210] Polystyrene 96-well plates were coated with 50 pl per well ofantibody 2TNF-H12 in PBS (10 μg/mL) and incubated in a humidifiedchamber at 4° C. overnight. The plates were washed with PBS and thenblocked with 5% nonfat-dry milk in PBS for 1 hour at room temperatureand washed with 0.1% BSA (bovine serum albumin) in PBS.

[0211] TNF standards were prepared from a stock solution of humanrecombinant TNF-α (R&D Systems, Minneapolis, Minn.). The concentrationof the standards in the assay began at 10 ng/mL followed by 6 half logserial dilutions.

[0212] Twenty five μL aliquots of the above culture supernatants or TNFstandards or only medium (control) were mixed with 25 μL aliquots ofbiotinylated monoclonal antibody 2TNF-H34 (2 μg/mL in PBS containing0.1% BSA) and then added to each well. The samples were incubated for 2hr at room temperature with gentle shaking and then washed 3 times with0.1% BSA in PBS. 50 μl of peroxidase-streptavidin (Zymed, S. SanFrancisco, Calif.) solution containing 0.416 μg/mL ofperoxidase-streptavidin and 0.1% BSA in PBS was added to each well. Thesamples were incubated for an additional 1 hr at room temperature andthen washed 4 times with 0.1% BSA in PBS. Fifty μL of O-phenylenediaminesolution (1 μg/mL O-phenylene-diamine and 0.03% hydrogen peroxide in0.2M citrate buffer pH 4.5) was added to each well and the samples wereincubated in the dark for 30 min., at room temperature. Optical densityof the sample and the reference were read at 450 nm and 650 nm,respectively. TNF-α levels were determined from a graph relating theoptical density at 450 nm to the concentration used.

[0213] The IC₅₀ value was defined as the concentration of the testcompound corresponding to half-maximal reduction in 450 nm absorbance.

Example 23

[0214] This example illustrates an in vivo assay to evaluate theinhibition of LPS-induced TNF-α production in mice (or rats).

[0215] The ability of the compounds of this invention to inhibit theTNF-α release, in vivo, was determined using a minor modification of themethods described in described in Zanetti, et. al., J. Immunol.,148:1890 (1992) and Sekut, et. al., J. Lab. Clin. Med., 124:813 (1994).

[0216] Female BALB/c mice weighing 18-21 grams (Charles River,Hollister, Calif.) were acclimated for one week. Groups containing 8mice each were dosed orally either with the test compounds suspended ordissolved in an aqueous vehicle containing 0.9% sodium chloride, 0.5%sodium carboxymethyl-cellulose, 0.4% polysorbate 80, 0.9% benzyl alcohol(CMC vehicle) or only vehicle (control group). After 30 min., the micewere injected intraperitoneally with 20 μg of LPS (Sigma, St. Louis,Mo.). After 1.5 h, the mice were sacrificed by CO₂ inhalation and bloodwas harvested by cardiocentesis. Blood was clarified by centrifugationat 15,600× g for 5 min., and sera were transferred to clean tubes andfrozen at −20° C. until analyzed for TNF-α by ELISA assay (BiosourceInternational, Camarillo, Calif. following the manufacturer's protocol.

[0217] The foregoing discussion of the invention has been presented forpurposes of illustration and description The foregoing is not intendedto limit the invention to the form or forms disclosed herein. Althoughthe description of the invention has included description of one or moreembodiments and certain variations and modifications, other variationsand modifications are within the scope of the invention, e.g., as may bewithin the skill and knowledge of those in the art, after understandingthe present disclosure. It is intended to obtain rights which includealternative embodiments to the extent permitted, including alternate,interchangeable and/or equivalent structures, functions, ranges or stepsto those claimed, whether or not such alternate, interchangeable and/orequivalent structures, functions, ranges or steps are disclosed herein,and without intending to publicly dedicate any patentable subjectmatter. All publications, patents, and patent applications cited hereinare hereby incorporated by reference in their entirety for all purposes.

What is claimed is:
 1. A compound of the formula:

a prodrug or a salt thereof, wherein: R¹ is hydrogen or alkyl; R² is—CR′R″—R^(a) (where R′ and R″ are hydrogen, hydroxyalkyl or alkyl withat least one being alkyl or hydroxyalkyl and R^(a) is hydroxyalkyl),R^(x)—S—R^(y)— (where R^(x) is alkyl and R^(y) is alkylene),alkoxy-substituted alkyl, heterocyclylalkyl or C₄-C₅ cycloalkyl, whereineach of the hydroxy group present in R² can be independently in the formof an ester, a carbamate, a carbonate, or a sulfonate derivative; or R¹and R² together with the nitrogen atom to which they are attached form aheterocyclyl group; R³ is hydrogen, alkyl, amino, monoalkylamino,dialkylamino, cycloalkyl, aryl, aralkyl, haloalkyl, heteroalkyl,cyanoalkyl, alkylene-C(O)—R (where R is hydrogen, alkyl, hydroxy,alkoxy, amino, monoalkylamino or dialkylamino) or acyl; and Ar¹ is aryl.2. The compound of claim 1 wherein Ar¹ is an optionally substitutedphenyl.
 3. The compound of claim 2, wherein Ar¹ is a phenyl groupindependently substituted with one or two halo, alkyl or methoxy groups.4. The compound of claim 3, wherein Ar¹ is 2-chlorophenyl,2-methylphenyl or 2-methoxyphenyl.
 5. The compound according to claim 4of the formula:


6. The compound according to claim 5, wherein R¹ is hydrogen or methyl.7. The compound according to claim 6, wherein R² is(1,1-dimethyl-2-hydroxy)ethyl, (1,2-dimethyl-2-hydroxy)propyl, or(1-substituted piperidin-4-yl)methyl, wherein each of the hydroxy grouppresent in R² can be independently in the form of an ester, a carbamate,a carbonate, or a sulfonate derivative.
 8. A composition comprising: (a)an excipient; and (b) a compound of the formula:

 a prodrug or a pharmaceutically acceptable salt thereof, wherein R¹ ishydrogen or alkyl; R² is —CR′R″—R^(a) (where R′ and R″ are hydrogen,hydroxyalkyl or alkyl with at least one being alkyl or hydroxyalkyl andR^(a) is hydroxyalkyl), R^(x)—S—R^(y)— (where R^(x) is alkyl and R^(y)is alkylene), alkoxy-substituted alkyl, heterocyclylalkyl or C₄-C₅cycloalkyl, wherein each of the hydroxy group present in R² can beindependently in the form of an ester, a carbamate, a carbonate, or asulfonate derivative; or R¹ and R² together with the nitrogen atom towhich they are attached forming a heterocyclyl group; <R³ is hydrogen,alkyl, amino, monoalkylamino, dialkylamino, cycloalkyl, aryl, aralkyl,haloalkyl, heteroalkyl, cyanoalkyl, alkylene-C(O)—R (where R ishydrogen, alkyl, hydroxy, alkoxy, amino, monoalkylamino or dialkylamino)or acyl; and Ar¹ is aryl.
 9. A method for preparing a compound of claim1, comprising the steps of contacting a compound of the formula Ig:

with an amine of the formula R¹R²NH under conditions sufficient toproduce a compound of Formula I:

wherein: R¹, R², R³ and Ar¹ are those defined in claim 1; L is a leavinggroup; n is an integer from 0 to 2; and R⁶ is an alkyl group.
 10. Themethod of claim 9, wherein n is
 1. 11. The method of claim 9 wherein nis
 2. 12. A method for treating a p38 mediated disorder comprisingadministering to a patient in need of such treatment, an effectiveamount of a compound of claim
 1. 13. The method of claim 12, whereinsaid p38 mediated disorder is arthritis, Crohns disease, Alzheimer'sdisease, irritable bowel syndrome, adult respiratory distress syndromeor chronic obstructive pulmonary disease.
 14. A process for producing apyrimidine of the formula:

comprising: (a) contacting an acetal of the formula NC—CH₂—C(OR^(a))₂,with an alkyl formate of the formula HCO₂R in the presence of acondensation base under conditions sufficient to produce a condensedproduct; and (b) contacting said condensed product with thiourea in thepresence of a cyclization base under conditions sufficient to producesaid pyrimidine of Formula II-c, wherein each of R and R^(a) isindependently alkyl.
 15. The process of claim 14, wherein saidcondensation base is a tert-butoxide.
 16. The process of claim 14,wherein said cyclization base is an alkoxide.
 17. A process forproducing a pyridopyrimidine of the formula:

comprising: (a) contacting a pyrimidine of the formula:

 with an alkylating agent of the formula R—X¹ in the presence of analkylating base under conditions sufficient to produce an alkylatedpyrimidine of the formula:

 and (b) contacting said alkylated pyrimidine of Formula II-d with anaryl acetate of the formula Ar¹—CH₂—CO₂R in the presence of acyclization base under conditions sufficient to produce saidpyridopyrimidine of Formula II-e  or (a) contacting said pyrimidine ofFormula II-c with said aryl acetate of the formula Ar¹—CH₂—CO₂R in thepresence of a cyclization base under conditions sufficient to produce athiol pyridopyrimidine of the formula:

 and (b) contacting said thiol pyridopyrimidine of Formula III with saidalkylating agent of the formula R—X¹ in the presence of an alkylatingbase under conditions sufficient to produce said pyridopyrimidine ofFormula II,  wherein X¹ is a leaving group; each R is independentlyalkyl; Ar¹ is aryl;
 18. The process of claim 17, wherein X¹ is halide.19. The process of claim 17 further comprising contacting saidpyridopyrimidine of Formula II with a nitrogen alkylating agent of theformula R³—X² under conditions sufficient to produce an N-substitutedpyridopyrimidine of the formula:

wherein R³ is alkyl, amino, monoalkylamino, dialkylamino, cycloalkyl,aralkyl, haloalkyl, heteroalkyl, cyanoalkyl, alkylene-C(O)—R′ (where R′is hydrogen, alkyl, hydroxy, alkoxy, amino, monoalkylamino ordialkylamino) or acyl; X² is a leaving group; and Ar¹ and R are thosedefined in claim
 17. 20. The process of claim 19, wherein X² is ahalogen.